戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 401611作成日:2026年10月27日

Phenol → 1-(2-Methoxy-ethoxy)-3-methyl-2-nitrobenzene

https://huagongshe.com/reaction/401611

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物Potassium CarbonateHCID 11430—
反応物3-Methyl-2-nitrophenolHCID 21026—
反応物2-Bromoethyl methyl etherHCID 80972—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-(2-Methoxy-ethoxy)-3-methyl-2-nitrobenzeneHCID 12855496—

反応条件

温度50 °C

反応手順

The required 1-(2-methoxy-ethoxy)-3-methyl-2-nitrobenzene was prepared from 3-methyl-2-nitrophenol. To a stirred solution of the phenol (2.0 g, 13.1 mmol) in DMF (65 mL) was added potassium carbonate (2.16 g, 15.7 mmol) and bromoethyl methyl ether (1.47 mL, 15.7 mmol) at room temperature. After the mixture was stirred at 50° C. for 48 h, water was added. The mixture was extracted with EtOAc (3×), washed with brine, dried over anhydrous MgSO4 filtered and evaporated. After chromatographic purification on silica gel, 1-(2-methoxy-ethoxy)-3-methyl-2-nitrobenzene was obtained in 85% yield (2.34 g). 1H NMR (500 MHz, CDCl3) δ 7.28 (1H, t, J=8.0 Hz), 6.89 (1H, d, J=9.0 Hz), 6.85 (1H, d, J=8.0 Hz), 4.19 (2H, t, J=4.5 Hz), 3.72 (2H, t, J=5.0 Hz), 3.41 (3H, s), 2.30 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741942B2
出典データセットuspto-grants-2014_06
ORD IDord-5b8c2a2be6f74fb8b7a7f609036c07b5
出典メモuspto-grants-2014_06